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首页> 外文期刊>Medicine. >Ophthalmoplegia associated with lung adenocarcinoma in a patient with the Lambert–Eaton myasthenic syndrome: A case report
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Ophthalmoplegia associated with lung adenocarcinoma in a patient with the Lambert–Eaton myasthenic syndrome: A case report

机译:兰伯特-伊顿肌无力综合症患者肺腺癌相关的眼肌麻痹:一例报告

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Rationale: The Lambert–Eaton myasthenic syndrome (LEMS) is a neuromuscular disease; its unique symptoms of LEMS include dry mouth with a metallic taste, constipation, and erectile dysfunction. As it is quite rare, isolated ocular muscle impairment associated with LEMS east to ignore. Patient concerns: A 65-year-old man presented with alternating ptosis and diplopia. Isolated ocular muscle impairment had lasted for 6 years, and the patient was initially diagnosed with ocular myasthenia gravis (MG). Treatment with azathioprine only slightly improved symptoms over the first 2 months; long-term treatment was not effective. Diagnoses: Dynamic observation of chest computed tomography images revealed a slowly progressing nodule in the lower lobe of the left lung. The subsequent pathologic examination following mass resection confirmed a diagnosis of lung adenocarcinoma. Interventions: The patient was ultimately diagnosed with the Lambert–Eaton myasthenic syndrome associated with pulmonary adenocarcinoma. Outcomes: Resection of the lung tumor relieved all symptoms. Lessons: Other causes of ocular MG symptoms should be considered when standard MG therapy is ineffective, especially the Lambert–Eaton myasthenic syndrome.
机译:理由:兰伯特-伊顿肌无力综合征(LEMS)是一种神经肌肉疾病; LEMS的独特症状包括口干,金属味,便秘和勃起功能障碍。由于很少见,与LEMS东部相关的孤立性眼肌损伤不容忽视。患者关注:一名65岁的男性出现上睑下垂和复视。孤立的眼肌损伤持续了6年,最初被诊断为重症肌无力(MG)。硫唑嘌呤治疗在最初的2个月中仅轻微改善了症状。长期治疗无效。诊断:对胸部计算机断层扫描图像的动态观察发现左肺下叶有一个缓慢进展的结节。肿块切除后的后续病理检查证实了肺腺癌的诊断。干预措施:该患者最终被诊断出患有肺腺癌的Lambert-Eaton重症肌无力综合征。结果:切除肺肿瘤可缓解所有症状。经验教训:当标准MG治疗无效时,应考虑其他眼部MG症状的原因,尤其是Lambert-Eaton肌无力综合症。

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